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methyl 4-oxo-1H-quinoline-7-carboxylate hydrochloride | 1018812-85-5

中文名称
——
中文别名
——
英文名称
methyl 4-oxo-1H-quinoline-7-carboxylate hydrochloride
英文别名
methyl 4-oxo-1H-quinoline-7-carboxylate;hydrochloride
methyl 4-oxo-1H-quinoline-7-carboxylate hydrochloride化学式
CAS
1018812-85-5
化学式
C11H9NO3*ClH
mdl
——
分子量
239.658
InChiKey
WRSUWVDAEYCQLP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.74
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    55.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    8-氯-4-氧代-1,4-二氢-喹啉-7-羧酸甲酯 在 palladium on activated charcoal 氢气 作用下, 以 乙醇 为溶剂, 20.0 ℃ 、300.01 kPa 条件下, 反应 8.0h, 以99%的产率得到methyl 4-oxo-1H-quinoline-7-carboxylate hydrochloride
    参考文献:
    名称:
    Strategic studies in the syntheses of novel 6,7-substituted quinolones and 7- or 6-substituted 1,6- and 1,7-naphthyridones
    摘要:
    This paper describes the different strategies devised and applied to overcome the selectivity issues in the syntheses of 6,7-disubstituted-1H-quinolin-4-one, 7-substituted-1H-1,6-naphthyridin-4-one and 6-substituted-1H-1,7-naphthyridin-4-one derivatives. They allowed us to improve the overall yields and the scating-up feasibility. Several examples illustrate these strategies with their advantages and drawbacks. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.01.055
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文献信息

  • Strategic studies in the syntheses of novel 6,7-substituted quinolones and 7- or 6-substituted 1,6- and 1,7-naphthyridones
    作者:Rémy Morgentin、Georges Pasquet、Pascal Boutron、Frédéric Jung、Maryannick Lamorlette、Mickaël Maudet、Patrick Plé
    DOI:10.1016/j.tet.2008.01.055
    日期:2008.3
    This paper describes the different strategies devised and applied to overcome the selectivity issues in the syntheses of 6,7-disubstituted-1H-quinolin-4-one, 7-substituted-1H-1,6-naphthyridin-4-one and 6-substituted-1H-1,7-naphthyridin-4-one derivatives. They allowed us to improve the overall yields and the scating-up feasibility. Several examples illustrate these strategies with their advantages and drawbacks. (C) 2008 Elsevier Ltd. All rights reserved.
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